CTRI/2023/03/050635
Not yet recruiting
Phase 3
Evaluation of visual, refractive outcome and changes in the ocular parameters after Eyecryl phakic IOL implementation in patients with moderate to high myopia and astigmatism: A prospective comparative study with EVO/EVO+ Visian implantable lenses
Prof MVanathi0 sites0 target enrollmentTBD
ConditionsHealth Condition 1: H521- Myopia
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: H521- Myopia
- Sponsor
- Prof MVanathi
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients with myopic astigmatism within a spherical equivalent (SE) range of \-3\.00 to \-20\.00 D and a minimum astigmatism of \-1\.00 D, stable refraction (0\.50 D or less change in the past 12 months),
- •2\.Minimum anterior chamber depth (ACD) from corneal endothelium of 2\.8 mm,
- •3\.Endothelial cell count of 2,500 cells/mm2
- •4\.Absence of corneal ectatic diseases, corneal scars,
- •5\.Absence of retinal pathologies
- •6\.Patients willing to give written informed consent and attend all follow\-up appointments
Exclusion Criteria
- •1\.Subject with previous intraocular or corneal surgery
- •2\.Subject with ocular condition like any cataract of any grade, glaucoma, severe dry eye, herpetic keratitis, uveitis
- •3\.Subject with systemic conditions like diabetes, collagen vascular diseases, immunosuppression
- •4\.Subject who is Pregnant or planning to start family, or lactating during the course of the evaluation
- •5\.Other condition associated with fluctuation of hormones
- •6\.Monocular subject
- •7\.Patient not willing to give written informed consent and attend all follow\-up appointments
Outcomes
Primary Outcomes
Not specified
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